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Bone Age Corresponds With Chronological Age at Type 1 Diabetes Onset in Youth

OBJECTIVE: To our knowledge, only two controversial articles have reported the study of bone age at diagnosis in diabetic children. The aim of this study was to compare chronological age with bone age and to evaluate the impact of A1C on bone age in children at diagnosis of type 1 diabetes. RESEARCH...

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Detalles Bibliográficos
Autores principales: Messaaoui, Anissa, Dorchy, Harry
Formato: Texto
Lenguaje:English
Publicado: American Diabetes Association 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2671119/
https://www.ncbi.nlm.nih.gov/pubmed/19228866
http://dx.doi.org/10.2337/dc08-2317
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author Messaaoui, Anissa
Dorchy, Harry
author_facet Messaaoui, Anissa
Dorchy, Harry
author_sort Messaaoui, Anissa
collection PubMed
description OBJECTIVE: To our knowledge, only two controversial articles have reported the study of bone age at diagnosis in diabetic children. The aim of this study was to compare chronological age with bone age and to evaluate the impact of A1C on bone age in children at diagnosis of type 1 diabetes. RESEARCH DESIGN AND METHODS: In 496 diabetic children, height was measured at diagnosis and height SD score was calculated using the British 1990 growth reference. Bone age was determined according to the Greulich and Pyle method, and A1C levels were measured. RESULTS: Participants' height was normal for age and sex. No significant differences were found between chronological age and bone age, and there was no correlation between Δ (bone age − chronological age) and A1C. CONCLUSIONS: This study showed that height and bone maturation among diabetic children are normal for age and sex and independent of A1C at diagnosis of type 1 diabetes.
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spelling pubmed-26711192010-05-01 Bone Age Corresponds With Chronological Age at Type 1 Diabetes Onset in Youth Messaaoui, Anissa Dorchy, Harry Diabetes Care Original Research OBJECTIVE: To our knowledge, only two controversial articles have reported the study of bone age at diagnosis in diabetic children. The aim of this study was to compare chronological age with bone age and to evaluate the impact of A1C on bone age in children at diagnosis of type 1 diabetes. RESEARCH DESIGN AND METHODS: In 496 diabetic children, height was measured at diagnosis and height SD score was calculated using the British 1990 growth reference. Bone age was determined according to the Greulich and Pyle method, and A1C levels were measured. RESULTS: Participants' height was normal for age and sex. No significant differences were found between chronological age and bone age, and there was no correlation between Δ (bone age − chronological age) and A1C. CONCLUSIONS: This study showed that height and bone maturation among diabetic children are normal for age and sex and independent of A1C at diagnosis of type 1 diabetes. American Diabetes Association 2009-05 2009-02-19 /pmc/articles/PMC2671119/ /pubmed/19228866 http://dx.doi.org/10.2337/dc08-2317 Text en © 2009 by the American Diabetes Association. https://creativecommons.org/licenses/by-nc-nd/3.0/Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0/ (https://creativecommons.org/licenses/by-nc-nd/3.0/) for details.
spellingShingle Original Research
Messaaoui, Anissa
Dorchy, Harry
Bone Age Corresponds With Chronological Age at Type 1 Diabetes Onset in Youth
title Bone Age Corresponds With Chronological Age at Type 1 Diabetes Onset in Youth
title_full Bone Age Corresponds With Chronological Age at Type 1 Diabetes Onset in Youth
title_fullStr Bone Age Corresponds With Chronological Age at Type 1 Diabetes Onset in Youth
title_full_unstemmed Bone Age Corresponds With Chronological Age at Type 1 Diabetes Onset in Youth
title_short Bone Age Corresponds With Chronological Age at Type 1 Diabetes Onset in Youth
title_sort bone age corresponds with chronological age at type 1 diabetes onset in youth
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2671119/
https://www.ncbi.nlm.nih.gov/pubmed/19228866
http://dx.doi.org/10.2337/dc08-2317
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